NP-MRD: Showing NP-Card for 2-hydroxy-n-{2-hydroxy-1-[(2s,3r)-3-tetradecyloxiran-2-yl]ethyl}tetracosanimidic acid (NP0256587)

Jump To Section:

Identification Spectra BioTaxonomy ChemoTaxonomy Physical properties Links References XML

Record Information

Version

2.0

Created at

2022-09-07 21:28:11 UTC

Updated at

2022-09-07 21:28:11 UTC

NP-MRD ID

NP0256587

Secondary Accession Numbers

None

Natural Product Identification

Common Name

2-hydroxy-n-{2-hydroxy-1-[(2s,3r)-3-tetradecyloxiran-2-yl]ethyl}tetracosanimidic acid

Description

Lactariamide A belongs to the class of organic compounds known as n-acyl amines. N-acyl amines are compounds containing a fatty acid moiety linked to an amine group through an ester linkage. 2-hydroxy-n-{2-hydroxy-1-[(2s,3r)-3-tetradecyloxiran-2-yl]ethyl}tetracosanimidic acid is found in Lactarius volemus. Based on a literature review very few articles have been published on Lactariamide A.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309072223282D          

 47 47  0  0  1  0            999 V2000
    0.5230  -16.0203    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2375  -15.6078    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9520  -16.0203    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6664  -15.6078    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3809  -16.0203    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0954  -15.6078    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8099  -16.0203    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5243  -15.6078    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2388  -16.0203    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.9533  -15.6078    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.6677  -16.0203    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.3822  -15.6078    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.0967  -16.0203    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.8112  -15.6078    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.5256  -16.0203    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.2401  -15.6078    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.9546  -16.0203    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.6690  -15.6078    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.3835  -16.0203    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.0980  -15.6078    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.8124  -16.0203    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   15.5269  -15.6078    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   16.2414  -16.0203    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   16.2414  -16.8453    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   16.9559  -15.6078    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   16.9559  -14.7828    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   17.6703  -16.0203    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   18.3848  -15.6078    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   19.0993  -16.0203    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   19.8137  -15.6078    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   18.3848  -14.7828    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   17.9723  -14.0684    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   18.7973  -14.0684    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   19.5118  -13.6559    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   19.5118  -12.8309    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   20.2262  -12.4184    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   20.2262  -11.5934    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   20.9407  -11.1809    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   20.9407  -10.3559    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   21.6552   -9.9434    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   21.6552   -9.1184    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   22.3697   -8.7059    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   22.3697   -7.8809    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   23.0841   -7.4684    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   23.0841   -6.6434    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   23.7986   -6.2309    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   23.7986   -5.4059    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  1  0  0  0  0
  3  4  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
 22 23  1  0  0  0  0
 23 24  1  0  0  0  0
 23 25  1  0  0  0  0
 25 26  1  0  0  0  0
 25 27  2  0  0  0  0
 27 28  1  4  0  0  0
 28 29  1  0  0  0  0
 29 30  1  0  0  0  0
 31 28  1  6  0  0  0
 31 32  1  0  0  0  0
 32 33  1  0  0  0  0
 31 33  1  0  0  0  0
 33 34  1  6  0  0  0
 34 35  1  0  0  0  0
 35 36  1  0  0  0  0
 36 37  1  0  0  0  0
 37 38  1  0  0  0  0
 38 39  1  0  0  0  0
 39 40  1  0  0  0  0
 40 41  1  0  0  0  0
 41 42  1  0  0  0  0
 42 43  1  0  0  0  0
 43 44  1  0  0  0  0
 44 45  1  0  0  0  0
 45 46  1  0  0  0  0
 46 47  1  0  0  0  0
M  END

     RDKit          3D

130130  0  0  0  0  0  0  0  0999 V2000
   16.8991    2.0033    0.3434 C   0  0  0  0  0  0  0  0  0  0  0  0
   17.0635    1.9327   -1.1647 C   0  0  0  0  0  0  0  0  0  0  0  0
   15.6817    1.6984   -1.7680 C   0  0  0  0  0  0  0  0  0  0  0  0
   15.1778    0.4055   -1.2033 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.7839    0.0418   -1.7291 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.3698   -1.2513   -1.1077 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.0293   -1.7446   -1.5206 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.8783   -0.8293   -1.2059 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.7660   -0.5405    0.2669 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.6022    0.3504    0.6075 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.2486   -0.2847    0.2053 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.0982   -1.5940    0.9231 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.9056   -2.3994    0.7250 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5530   -1.9728    1.0720 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8868   -0.8446    0.4540 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4408   -0.7097    1.0144 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5258   -0.4168    2.4632 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3055   -0.1716    3.2494 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2809   -1.2115    3.4469 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5308   -1.7351    2.2861 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2213   -0.5962    1.5998 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9777   -1.2080    0.4466 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7847   -0.1936   -0.2681 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.9199    0.7904   -0.7583 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7095    0.4784    0.6775 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1338   -0.0211    1.8784 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1679    1.6495    0.3366 N   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0527    2.4085    1.1364 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.6078    3.8751    1.2350 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5598    4.4719   -0.0016 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4980    2.3868    0.9087 C   0  0  2  0  0  0  0  0  0  0  0  0
   -6.2515    1.2096    0.9741 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3375    2.0955   -0.2017 C   0  0  2  0  0  0  0  0  0  0  0  0
   -6.1311    1.3067   -1.4351 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8141   -0.1123   -1.3367 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.5895   -1.1417   -0.6779 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.9064   -1.5804   -1.0212 C   0  0  0  0  0  0  0  0  0  0  0  0
   -9.1983   -0.9115   -0.9488 C   0  0  0  0  0  0  0  0  0  0  0  0
   -9.4960    0.3220   -1.6638 C   0  0  0  0  0  0  0  0  0  0  0  0
  -10.8661    0.8834   -1.6332 C   0  0  0  0  0  0  0  0  0  0  0  0
  -12.0258    0.2081   -2.1815 C   0  0  0  0  0  0  0  0  0  0  0  0
  -12.4573   -1.1184   -1.6892 C   0  0  0  0  0  0  0  0  0  0  0  0
  -12.7619   -1.2106   -0.2306 C   0  0  0  0  0  0  0  0  0  0  0  0
  -13.8654   -0.3353    0.2618 C   0  0  0  0  0  0  0  0  0  0  0  0
  -15.1842   -0.6175   -0.3793 C   0  0  0  0  0  0  0  0  0  0  0  0
  -16.2172    0.3284    0.2235 C   0  0  0  0  0  0  0  0  0  0  0  0
  -15.7690    1.7370   -0.0688 C   0  0  0  0  0  0  0  0  0  0  0  0
   17.8064    2.4775    0.7682 H   0  0  0  0  0  0  0  0  0  0  0  0
   16.8905    0.9346    0.7051 H   0  0  0  0  0  0  0  0  0  0  0  0
   15.9599    2.4756    0.6562 H   0  0  0  0  0  0  0  0  0  0  0  0
   17.5479    2.8348   -1.5816 H   0  0  0  0  0  0  0  0  0  0  0  0
   17.6604    1.0291   -1.4021 H   0  0  0  0  0  0  0  0  0  0  0  0
   15.0045    2.5273   -1.4661 H   0  0  0  0  0  0  0  0  0  0  0  0
   15.7358    1.6652   -2.8573 H   0  0  0  0  0  0  0  0  0  0  0  0
   15.8826   -0.4150   -1.4855 H   0  0  0  0  0  0  0  0  0  0  0  0
   15.0803    0.4578   -0.0983 H   0  0  0  0  0  0  0  0  0  0  0  0
   13.8237   -0.0656   -2.8321 H   0  0  0  0  0  0  0  0  0  0  0  0
   13.1299    0.8956   -1.4834 H   0  0  0  0  0  0  0  0  0  0  0  0
   13.5029   -1.2443    0.0102 H   0  0  0  0  0  0  0  0  0  0  0  0
   14.1120   -2.0265   -1.4659 H   0  0  0  0  0  0  0  0  0  0  0  0
   12.0622   -1.8285   -2.6491 H   0  0  0  0  0  0  0  0  0  0  0  0
   11.8817   -2.7669   -1.1458 H   0  0  0  0  0  0  0  0  0  0  0  0
   10.9348    0.1076   -1.7675 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.9606   -1.3588   -1.5349 H   0  0  0  0  0  0  0  0  0  0  0  0
   11.6829    0.0713    0.5522 H   0  0  0  0  0  0  0  0  0  0  0  0
   10.7364   -1.4230    0.9106 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.6792    1.3678    0.1640 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.5679    0.4747    1.7087 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.2655   -0.4741   -0.8734 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.5154    0.4911    0.4849 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.4314   -1.5082    1.9974 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.9618   -2.2244    0.4958 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.8989   -2.6875   -0.3932 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.1264   -3.4286    1.1790 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.5733   -1.8264    2.2109 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8490   -2.8678    0.9974 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6843   -1.0500   -0.6418 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2811    0.1675    0.5850 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9418   -1.6555    0.7705 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9945    0.1587    0.4786 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2886    0.4186    2.6444 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.0439   -1.2824    3.0239 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6557    0.2061    4.2772 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8373    0.7817    2.8343 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5337   -0.8547    4.2359 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7330   -2.1414    3.9482 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2783   -2.4356    2.7237 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0827   -2.3761    1.6157 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8944   -0.1903    2.3717 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4863    0.1733    1.2412 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2608   -1.6656   -0.2753 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6471   -2.0226    0.8091 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3302   -0.5888   -1.1506 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3714    1.6474   -0.8580 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6906   -0.8353    1.9987 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8770    2.0374    2.2089 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3844    4.3719    1.8457 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6535    3.9528    1.8036 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3664    3.7607   -0.6596 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0014    3.1526    1.6528 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.3398    2.6556   -0.2370 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2338    1.7628   -2.0261 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.9531    1.4810   -2.1676 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7027   -0.1865   -1.0842 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7251   -0.4487   -2.4714 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9150   -2.1098   -0.7727 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4576   -1.0218    0.4735 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.8133   -2.0740   -2.0998 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.1046   -2.6191   -0.4673 H   0  0  0  0  0  0  0  0  0  0  0  0
   -9.9724   -1.7248   -1.1005 H   0  0  0  0  0  0  0  0  0  0  0  0
   -9.3379   -0.6571    0.1849 H   0  0  0  0  0  0  0  0  0  0  0  0
   -9.0344    0.3198   -2.6702 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.8990    1.1427   -1.0961 H   0  0  0  0  0  0  0  0  0  0  0  0
  -10.7933    1.8980   -2.1470 H   0  0  0  0  0  0  0  0  0  0  0  0
  -11.1298    1.2037   -0.5702 H   0  0  0  0  0  0  0  0  0  0  0  0
  -12.9180    0.8988   -1.9786 H   0  0  0  0  0  0  0  0  0  0  0  0
  -12.0571    0.1641   -3.3085 H   0  0  0  0  0  0  0  0  0  0  0  0
  -11.9416   -2.0031   -2.0432 H   0  0  0  0  0  0  0  0  0  0  0  0
  -13.5110   -1.2586   -2.1789 H   0  0  0  0  0  0  0  0  0  0  0  0
  -11.8571   -1.0915    0.4086 H   0  0  0  0  0  0  0  0  0  0  0  0
  -13.0854   -2.2760   -0.0394 H   0  0  0  0  0  0  0  0  0  0  0  0
  -13.6414    0.7471    0.1802 H   0  0  0  0  0  0  0  0  0  0  0  0
  -13.9835   -0.5533    1.3514 H   0  0  0  0  0  0  0  0  0  0  0  0
  -15.2020   -0.4075   -1.4744 H   0  0  0  0  0  0  0  0  0  0  0  0
  -15.4930   -1.6629   -0.1943 H   0  0  0  0  0  0  0  0  0  0  0  0
  -17.1835    0.1271   -0.2666 H   0  0  0  0  0  0  0  0  0  0  0  0
  -16.3290    0.1414    1.3124 H   0  0  0  0  0  0  0  0  0  0  0  0
  -15.1594    1.7693   -0.9878 H   0  0  0  0  0  0  0  0  0  0  0  0
  -16.6306    2.4316   -0.1912 H   0  0  0  0  0  0  0  0  0  0  0  0
  -15.1906    2.1258    0.7813 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  1  0
  4  5  1  0
  5  6  1  0
  6  7  1  0
  7  8  1  0
  8  9  1  0
  9 10  1  0
 10 11  1  0
 11 12  1  0
 12 13  1  0
 13 14  1  0
 14 15  1  0
 15 16  1  0
 16 17  1  0
 17 18  1  0
 18 19  1  0
 19 20  1  0
 20 21  1  0
 21 22  1  0
 22 23  1  0
 23 24  1  0
 23 25  1  0
 25 26  1  0
 25 27  2  0
 27 28  1  0
 28 29  1  0
 29 30  1  0
 28 31  1  0
 31 32  1  0
 32 33  1  0
 33 34  1  0
 34 35  1  0
 35 36  1  0
 36 37  1  0
 37 38  1  0
 38 39  1  0
 39 40  1  0
 40 41  1  0
 41 42  1  0
 42 43  1  0
 43 44  1  0
 44 45  1  0
 45 46  1  0
 46 47  1  0
 33 31  1  0
  1 48  1  0
  1 49  1  0
  1 50  1  0
  2 51  1  0
  2 52  1  0
  3 53  1  0
  3 54  1  0
  4 55  1  0
  4 56  1  0
  5 57  1  0
  5 58  1  0
  6 59  1  0
  6 60  1  0
  7 61  1  0
  7 62  1  0
  8 63  1  0
  8 64  1  0
  9 65  1  0
  9 66  1  0
 10 67  1  0
 10 68  1  0
 11 69  1  0
 11 70  1  0
 12 71  1  0
 12 72  1  0
 13 73  1  0
 13 74  1  0
 14 75  1  0
 14 76  1  0
 15 77  1  0
 15 78  1  0
 16 79  1  0
 16 80  1  0
 17 81  1  0
 17 82  1  0
 18 83  1  0
 18 84  1  0
 19 85  1  0
 19 86  1  0
 20 87  1  0
 20 88  1  0
 21 89  1  0
 21 90  1  0
 22 91  1  0
 22 92  1  0
 23 93  1  6
 24 94  1  0
 26 95  1  0
 28 96  1  1
 29 97  1  0
 29 98  1  0
 30 99  1  0
 31100  1  1
 33101  1  6
 34102  1  0
 34103  1  0
 35104  1  0
 35105  1  0
 36106  1  0
 36107  1  0
 37108  1  0
 37109  1  0
 38110  1  0
 38111  1  0
 39112  1  0
 39113  1  0
 40114  1  0
 40115  1  0
 41116  1  0
 41117  1  0
 42118  1  0
 42119  1  0
 43120  1  0
 43121  1  0
 44122  1  0
 44123  1  0
 45124  1  0
 45125  1  0
 46126  1  0
 46127  1  0
 47128  1  0
 47129  1  0
 47130  1  0
M  END


  Mrv1652309072223282D          

 47 47  0  0  1  0            999 V2000
    0.5230  -16.0203    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2375  -15.6078    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9520  -16.0203    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6664  -15.6078    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3809  -16.0203    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0954  -15.6078    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8099  -16.0203    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5243  -15.6078    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2388  -16.0203    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.9533  -15.6078    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.6677  -16.0203    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.3822  -15.6078    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.0967  -16.0203    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.8112  -15.6078    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.5256  -16.0203    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.2401  -15.6078    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.9546  -16.0203    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.6690  -15.6078    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.3835  -16.0203    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.0980  -15.6078    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.8124  -16.0203    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   15.5269  -15.6078    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   16.2414  -16.0203    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   16.2414  -16.8453    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   16.9559  -15.6078    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   16.9559  -14.7828    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   17.6703  -16.0203    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   18.3848  -15.6078    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   19.0993  -16.0203    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   19.8137  -15.6078    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   18.3848  -14.7828    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   17.9723  -14.0684    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   18.7973  -14.0684    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   19.5118  -13.6559    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   19.5118  -12.8309    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   20.2262  -12.4184    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   20.2262  -11.5934    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   20.9407  -11.1809    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   20.9407  -10.3559    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   21.6552   -9.9434    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   21.6552   -9.1184    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   22.3697   -8.7059    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   22.3697   -7.8809    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   23.0841   -7.4684    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   23.0841   -6.6434    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   23.7986   -6.2309    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   23.7986   -5.4059    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  1  0  0  0  0
  3  4  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
 22 23  1  0  0  0  0
 23 24  1  0  0  0  0
 23 25  1  0  0  0  0
 25 26  1  0  0  0  0
 25 27  2  0  0  0  0
 27 28  1  4  0  0  0
 28 29  1  0  0  0  0
 29 30  1  0  0  0  0
 31 28  1  6  0  0  0
 31 32  1  0  0  0  0
 32 33  1  0  0  0  0
 31 33  1  0  0  0  0
 33 34  1  6  0  0  0
 34 35  1  0  0  0  0
 35 36  1  0  0  0  0
 36 37  1  0  0  0  0
 37 38  1  0  0  0  0
 38 39  1  0  0  0  0
 39 40  1  0  0  0  0
 40 41  1  0  0  0  0
 41 42  1  0  0  0  0
 42 43  1  0  0  0  0
 43 44  1  0  0  0  0
 44 45  1  0  0  0  0
 45 46  1  0  0  0  0
 46 47  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0256587

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CCCCCCCCCCCCCCCCCCCCCCC(O)C(O)=NC(CO)[C@@H]1O[C@@H]1CCCCCCCCCCCCCC

> <INCHI_IDENTIFIER>
InChI=1S/C42H83NO4/c1-3-5-7-9-11-13-15-17-18-19-20-21-22-23-24-25-27-29-31-33-35-39(45)42(46)43-38(37-44)41-40(47-41)36-34-32-30-28-26-16-14-12-10-8-6-4-2/h38-41,44-45H,3-37H2,1-2H3,(H,43,46)/t38?,39?,40-,41+/m1/s1

> <INCHI_KEY>
LZQIWGKTNAQMJH-QXLYETOESA-N

> <FORMULA>
C42H83NO4

> <MOLECULAR_WEIGHT>
666.129

> <EXACT_MASS>
665.632210157

> <JCHEM_ACCEPTOR_COUNT>
5

> <JCHEM_ATOM_COUNT>
130

> <JCHEM_AVERAGE_POLARIZABILITY>
90.46201496906106

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
3

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
2-hydroxy-N-{2-hydroxy-1-[(2S,3R)-3-tetradecyloxiran-2-yl]ethyl}tetracosanimidic acid

> <JCHEM_LOGP>
14.663256832000002

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
1

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
14.313251879041921

> <JCHEM_PKA_STRONGEST_ACIDIC>
4.228199538999564

> <JCHEM_PKA_STRONGEST_BASIC>
2.0178603402824487

> <JCHEM_POLAR_SURFACE_AREA>
85.58000000000001

> <JCHEM_REFRACTIVITY>
201.4864

> <JCHEM_ROTATABLE_BOND_COUNT>
38

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
2-hydroxy-N-{2-hydroxy-1-[(2S,3R)-3-tetradecyloxiran-2-yl]ethyl}tetracosanimidic acid

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 07-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   07-SEP-22         0                                  
HETATM    1  C   UNK     0       0.976 -29.905   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       2.310 -29.135   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       3.644 -29.905   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       4.977 -29.135   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       6.311 -29.905   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       7.645 -29.135   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       8.978 -29.905   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      10.312 -29.135   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      11.646 -29.905   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      12.979 -29.135   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      14.313 -29.905   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      15.647 -29.135   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      16.980 -29.905   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      18.314 -29.135   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      19.648 -29.905   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      20.982 -29.135   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      22.315 -29.905   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      23.649 -29.135   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      24.983 -29.905   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      26.316 -29.135   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      27.650 -29.905   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      28.984 -29.135   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0      30.317 -29.905   0.000  0.00  0.00           C+0
HETATM   24  O   UNK     0      30.317 -31.445   0.000  0.00  0.00           O+0
HETATM   25  C   UNK     0      31.651 -29.135   0.000  0.00  0.00           C+0
HETATM   26  O   UNK     0      31.651 -27.595   0.000  0.00  0.00           O+0
HETATM   27  N   UNK     0      32.985 -29.905   0.000  0.00  0.00           N+0
HETATM   28  C   UNK     0      34.318 -29.135   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0      35.652 -29.905   0.000  0.00  0.00           C+0
HETATM   30  O   UNK     0      36.986 -29.135   0.000  0.00  0.00           O+0
HETATM   31  C   UNK     0      34.318 -27.595   0.000  0.00  0.00           C+0
HETATM   32  O   UNK     0      33.548 -26.261   0.000  0.00  0.00           O+0
HETATM   33  C   UNK     0      35.088 -26.261   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0      36.422 -25.491   0.000  0.00  0.00           C+0
HETATM   35  C   UNK     0      36.422 -23.951   0.000  0.00  0.00           C+0
HETATM   36  C   UNK     0      37.756 -23.181   0.000  0.00  0.00           C+0
HETATM   37  C   UNK     0      37.756 -21.641   0.000  0.00  0.00           C+0
HETATM   38  C   UNK     0      39.089 -20.871   0.000  0.00  0.00           C+0
HETATM   39  C   UNK     0      39.089 -19.331   0.000  0.00  0.00           C+0
HETATM   40  C   UNK     0      40.423 -18.561   0.000  0.00  0.00           C+0
HETATM   41  C   UNK     0      40.423 -17.021   0.000  0.00  0.00           C+0
HETATM   42  C   UNK     0      41.757 -16.251   0.000  0.00  0.00           C+0
HETATM   43  C   UNK     0      41.757 -14.711   0.000  0.00  0.00           C+0
HETATM   44  C   UNK     0      43.090 -13.941   0.000  0.00  0.00           C+0
HETATM   45  C   UNK     0      43.090 -12.401   0.000  0.00  0.00           C+0
HETATM   46  C   UNK     0      44.424 -11.631   0.000  0.00  0.00           C+0
HETATM   47  C   UNK     0      44.424 -10.091   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4                                                       
CONECT    4    3    5                                                       
CONECT    5    4    6                                                       
CONECT    6    5    7                                                       
CONECT    7    6    8                                                       
CONECT    8    7    9                                                       
CONECT    9    8   10                                                       
CONECT   10    9   11                                                       
CONECT   11   10   12                                                       
CONECT   12   11   13                                                       
CONECT   13   12   14                                                       
CONECT   14   13   15                                                       
CONECT   15   14   16                                                       
CONECT   16   15   17                                                       
CONECT   17   16   18                                                       
CONECT   18   17   19                                                       
CONECT   19   18   20                                                       
CONECT   20   19   21                                                       
CONECT   21   20   22                                                       
CONECT   22   21   23                                                       
CONECT   23   22   24   25                                                  
CONECT   24   23                                                            
CONECT   25   23   26   27                                                  
CONECT   26   25                                                            
CONECT   27   25   28                                                       
CONECT   28   27   29   31                                                  
CONECT   29   28   30                                                       
CONECT   30   29                                                            
CONECT   31   28   32   33                                                  
CONECT   32   31   33                                                       
CONECT   33   32   31   34                                                  
CONECT   34   33   35                                                       
CONECT   35   34   36                                                       
CONECT   36   35   37                                                       
CONECT   37   36   38                                                       
CONECT   38   37   39                                                       
CONECT   39   38   40                                                       
CONECT   40   39   41                                                       
CONECT   41   40   42                                                       
CONECT   42   41   43                                                       
CONECT   43   42   44                                                       
CONECT   44   43   45                                                       
CONECT   45   44   46                                                       
CONECT   46   45   47                                                       
CONECT   47   46                                                            
MASTER        0    0    0    0    0    0    0    0   47    0   94    0
END

View in JSmol

Synonyms

Value	Source
N-2'-Hydroxytetracosanoyl-2-amino-3,4-epoxyoctadecan-1-ol	MeSH

Chemical Formula

C₄₂H₈₃NO₄

Average Mass

666.1290 Da

Monoisotopic Mass

665.63221 Da

IUPAC Name

2-hydroxy-N-{2-hydroxy-1-[(2S,3R)-3-tetradecyloxiran-2-yl]ethyl}tetracosanimidic acid

Traditional Name

2-hydroxy-N-{2-hydroxy-1-[(2S,3R)-3-tetradecyloxiran-2-yl]ethyl}tetracosanimidic acid

CAS Registry Number

Not Available

SMILES

CCCCCCCCCCCCCCCCCCCCCCC(O)C(O)=NC(CO)[C@@H]1O[C@@H]1CCCCCCCCCCCCCC

InChI Identifier

InChI=1S/C42H83NO4/c1-3-5-7-9-11-13-15-17-18-19-20-21-22-23-24-25-27-29-31-33-35-39(45)42(46)43-38(37-44)41-40(47-41)36-34-32-30-28-26-16-14-12-10-8-6-4-2/h38-41,44-45H,3-37H2,1-2H3,(H,43,46)/t38?,39?,40-,41+/m1/s1

InChI Key

LZQIWGKTNAQMJH-QXLYETOESA-N

Experimental Spectra

Not Available

Predicted Spectra

Spectrum Type	Description	Depositor ID	Depositor Organization	Depositor	Deposition Date	View
1D NMR	¹³C NMR Spectrum (1D, 25 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 252 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 50 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 75 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 101 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 126 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 151 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 176 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 201 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 226 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum

Chemical Shift Submissions

Not Available

Species

Species of Origin

Species Name	Source	Reference
Lactarius volemus	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as n-acyl amines. N-acyl amines are compounds containing a fatty acid moiety linked to an amine group through an ester linkage.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Fatty Acyls

Sub Class

Fatty amides

Direct Parent

N-acyl amines

Alternative Parents

Substituents

Monosaccharide
N-acyl-amine
Carboxamide group
Secondary alcohol
Secondary carboxylic acid amide
Carboxylic acid derivative
Dialkyl ether
Oxirane
Ether
Oxacycle
Organoheterocyclic compound
Organic oxide
Organic oxygen compound
Organic nitrogen compound
Carbonyl group
Organonitrogen compound
Organooxygen compound
Primary alcohol
Hydrocarbon derivative
Alcohol
Aliphatic heteromonocyclic compound

Molecular Framework

Aliphatic heteromonocyclic compounds

External Descriptors

Not Available

Physical Properties

State

Not Available

Experimental Properties

Property	Value	Reference
Melting Point	Not Available	Not Available
Boiling Point	Not Available	Not Available
Water Solubility	Not Available	Not Available
LogP	Not Available	Not Available

Predicted Properties

Property	Value	Source
logP	14.66	ChemAxon
pKa (Strongest Acidic)	4.23	ChemAxon
pKa (Strongest Basic)	2.02	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	5	ChemAxon
Hydrogen Donor Count	3	ChemAxon
Polar Surface Area	85.58 Å²	ChemAxon
Rotatable Bond Count	38	ChemAxon
Refractivity	201.49 m³·mol⁻¹	ChemAxon
Polarizability	90.46 Å³	ChemAxon
Number of Rings	1	ChemAxon
Bioavailability	No	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	No	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	No	ChemAxon

External Links

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

Not Available

KNApSAcK ID

C00046070

Chemspider ID

9942223

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

11767538

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 2-hydroxy-n-{2-hydroxy-1-[(2s,3r)-3-tetradecyloxiran-2-yl]ethyl}tetracosanimidic acid (NP0256587)

MOL for NP0256587 (2-hydroxy-n-{2-hydroxy-1-[(2s,3r)-3-tetradecyloxiran-2-yl]ethyl}tetracosanimidic acid)

3D MOL for NP0256587 (2-hydroxy-n-{2-hydroxy-1-[(2s,3r)-3-tetradecyloxiran-2-yl]ethyl}tetracosanimidic acid)

3D SDF for NP0256587 (2-hydroxy-n-{2-hydroxy-1-[(2s,3r)-3-tetradecyloxiran-2-yl]ethyl}tetracosanimidic acid)

3D-SDF for NP0256587 (2-hydroxy-n-{2-hydroxy-1-[(2s,3r)-3-tetradecyloxiran-2-yl]ethyl}tetracosanimidic acid)

PDB for NP0256587 (2-hydroxy-n-{2-hydroxy-1-[(2s,3r)-3-tetradecyloxiran-2-yl]ethyl}tetracosanimidic acid)

3D PDB for NP0256587 (2-hydroxy-n-{2-hydroxy-1-[(2s,3r)-3-tetradecyloxiran-2-yl]ethyl}tetracosanimidic acid)

SMILES for NP0256587 (2-hydroxy-n-{2-hydroxy-1-[(2s,3r)-3-tetradecyloxiran-2-yl]ethyl}tetracosanimidic acid)

INCHI for NP0256587 (2-hydroxy-n-{2-hydroxy-1-[(2s,3r)-3-tetradecyloxiran-2-yl]ethyl}tetracosanimidic acid)

Structure for NP0256587 (2-hydroxy-n-{2-hydroxy-1-[(2s,3r)-3-tetradecyloxiran-2-yl]ethyl}tetracosanimidic acid)

3D Structure for NP0256587 (2-hydroxy-n-{2-hydroxy-1-[(2s,3r)-3-tetradecyloxiran-2-yl]ethyl}tetracosanimidic acid)